Non-conventional yeasts are increasingly being investigated and used as producers in biotechnological processes which often offer advantages in comparison to traditional and well-established systems. Most biotechnologically interesting non-conventional yeasts belong to the subphylum, including those already in use (, etc.), as well as those that are promising but as yet insufficiently characterized. Moreover, for many of these yeasts the basic tools of genetic engineering needed for strain construction, including a procedure for efficient genetic transformation, heterologous protein expression and precise genetic modification, are lacking. The first aim of this study was to construct a set of integrative and replicative plasmids which can be used in various yeasts across the subphylum. Additionally, we demonstrate here that the electroporation procedure we developed earlier for transformation of can be applied in various yeasts which, together with the constructed plasmids, makes a solid starting point when approaching a transformation of yeasts form the subphylum. To provide a proof of principle, we successfully transformed three species from the genus (, and ) with high efficiencies (up to 8 × 10 in case of illegitimate integration of non-homologous linear DNA and up to 4.7 × 10 in case of replicative plasmid). For the latter two species this is the first reported genetic transformation. Moreover, we found that a plasmid carrying replication origin from can be used as a replicative plasmid for these three species.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9146037 | PMC |
http://dx.doi.org/10.3390/jof8050531 | DOI Listing |
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